Canonical Allele Identifier: CA1430709642

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604694_194604695delinsCA , CM000665.2:g.194604694_194604695delinsCA	GRCh38
NC_000003.11:g.194325423_194325424delinsCA , CM000665.1:g.194325423_194325424delinsCA	GRCh37
NC_000003.10:g.195806712_195806713delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1018-250_1018-249delinsTG MANE Select	ENSP00000333355.6:n.1018-250_1018-249delinsTG
ENST00000347147.8:c.1018-250_1018-249delinsTG	ENSP00000333355.6:n.1018-250_1018-249delinsTG
ENST00000381975.7:c.1018-254_1018-253delinsTG	ENSP00000371402.3:n.1018-254_1018-253delinsTG
ENST00000392432.6:c.1159-250_1159-249delinsTG	ENSP00000376227.2:n.1159-250_1159-249delinsTG
ENST00000419280.5:c.*314-250_*314-249delinsTG	ENSP00000414077.1:n.*314-250_*314-249delinsTG
ENST00000429560.1:c.214-254_214-253delinsTG	ENSP00000403053.1:n.214-254_214-253delinsTG
ENST00000432352.5:c.292-250_292-249delinsTG	ENSP00000409963.1:n.292-250_292-249delinsTG
ENST00000452358.5:c.517-250_517-249delinsTG	ENSP00000414333.1:n.517-250_517-249delinsTG
ENST00000467284.1:n.64-250_64-249delinsTG
ENST00000473092.5:c.1018-250_1018-249delinsTG	ENSP00000418674.1:n.1018-250_1018-249delinsTG
ENST00000477651.5:n.782-250_782-249delinsTG
NM_001011655.2:c.1018-250_1018-249delinsTG	NP_001011655.1:n.1018-250_1018-249delinsTG
NM_001166305.1:c.1159-250_1159-249delinsTG	NP_001159777.1:n.1159-250_1159-249delinsTG
NM_001166306.1:c.1018-254_1018-253delinsTG	NP_001159778.1:n.1018-254_1018-253delinsTG
NM_138399.4:c.1018-250_1018-249delinsTG	NP_612408.3:n.1018-250_1018-249delinsTG
XM_005269371.3:c.1018-250_1018-249delinsTG	XP_005269428.1:n.1018-250_1018-249delinsTG
XM_011513318.1:c.1168-250_1168-249delinsTG	XP_011511620.1:n.1168-250_1168-249delinsTG
XM_011513319.1:c.1105-250_1105-249delinsTG	XP_011511621.1:n.1105-250_1105-249delinsTG
XM_011513320.1:c.1216-250_1216-249delinsTG	XP_011511622.1:n.1216-250_1216-249delinsTG
XM_011513321.1:c.1084-250_1084-249delinsTG	XP_011511623.1:n.1084-250_1084-249delinsTG
XM_011513322.1:c.1075-250_1075-249delinsTG	XP_011511624.1:n.1075-250_1075-249delinsTG
XM_011513323.1:c.913-250_913-249delinsTG	XP_011511625.1:n.913-250_913-249delinsTG
XM_005269371.4:c.1018-250_1018-249delinsTG	XP_005269428.1:n.1018-250_1018-249delinsTG
XM_011513318.2:c.1168-250_1168-249delinsTG	XP_011511620.1:n.1168-250_1168-249delinsTG
XM_011513319.2:c.1105-250_1105-249delinsTG	XP_011511621.1:n.1105-250_1105-249delinsTG
XM_011513320.2:c.1216-250_1216-249delinsTG	XP_011511622.1:n.1216-250_1216-249delinsTG
XM_011513321.2:c.1084-250_1084-249delinsTG	XP_011511623.1:n.1084-250_1084-249delinsTG
XM_011513322.2:c.1075-250_1075-249delinsTG	XP_011511624.1:n.1075-250_1075-249delinsTG
XM_017007517.1:c.1027-250_1027-249delinsTG	XP_016863006.1:n.1027-250_1027-249delinsTG
XM_017007518.1:c.1027-250_1027-249delinsTG	XP_016863007.1:n.1027-250_1027-249delinsTG
NM_001011655.3:c.1018-250_1018-249delinsTG MANE Select	NP_001011655.1:n.1018-250_1018-249delinsTG
NM_001166305.2:c.1159-250_1159-249delinsTG	NP_001159777.1:n.1159-250_1159-249delinsTG
NM_001166306.2:c.1018-254_1018-253delinsTG	NP_001159778.1:n.1018-254_1018-253delinsTG
NM_138399.5:c.1018-250_1018-249delinsTG	NP_612408.3:n.1018-250_1018-249delinsTG